Lista de obras -

A PEX6-defective peroxisomal biogenesis disorder with severe phenotype in an infant, versus mild phenotype resembling Usher syndrome in the affected parents

artículo científico publicado en 2002

A role for the peroxisomal 3-ketoacyl-CoA thiolase B enzyme in the control of PPARα-mediated upregulation of SREBP-2 target genes in the liver.

artículo científico publicado en 2011

Age-associated differential microRNA levels in human follicular fluid reveal pathways potentially determining fertility and success of in vitro fertilization.

artículo científico publicado en 2014

Expression of calcium-sensing receptor in quail granulosa explants: a key to survival during folliculogenesis

artículo científico publicado en 2010

Fine structure of the statocyst sensilla of the mysid shrimp Neomysis integer (Leach, 1814) (Crustacea, Mysidacea)

artículo científico publicado en 1985

Human mevalonate pyrophosphate decarboxylase is localized in the cytosol

artículo científico publicado en 2004

Human peroxisomal disorders ⬇️

artículo científico publicado el 1 de junio de 2003

Immunohistochemical demonstration of the amphetamine derivatives 3,4-methylenedioxymethamphetamine (MDMA) and 3,4-methylenedioxyamphetamine (MDA) in human post-mortem brain tissues and the pituitary gland

artículo científico publicado en 2003

Inborn errors of metabolism in the biosynthesis and remodelling of phospholipids

artículo científico publicado en 2014

Mevalonate kinase is a cytosolic enzyme in humans

artículo científico publicado en 2004

Mitochondria in peroxisome-deficient hepatocytes exhibit impaired respiration, depleted DNA, and PGC-1α independent proliferation

artículo científico publicado en 2014

Mitochondrial disruption in peroxisome deficient cells is hepatocyte selective but is not mediated by common hepatic peroxisomal metabolites

artículo científico publicado en 2017

Mitochondrial mosaics in the liver of 3 infants with mtDNA defects

artículo científico publicado en 2009

Modified peroxisomes in primary hepatocyte cultures.

artículo científico publicado en 2003

Morphogenesis during molting of the setae in the statocyst sensilla of the mysid shrimp Neomysis integer (Leach, 1814) (crustacea, mysidacea)

artículo científico publicado en 1986

Neocortical and cerebellar developmental abnormalities in conditions of selective elimination of peroxisomes from brain or from liver

artículo científico publicado en 2007

Peroxisome deficient aP2-Pex5 knockout mice display impaired white adipocyte and muscle function concomitant with reduced adrenergic tone

artículo científico publicado en 2012

Peroxisome mosaics.

artículo científico publicado en 2003

Peroxisomes during development and in distinct cell types.

artículo científico publicado en 2003

Peroxisomes in zebrafish: distribution pattern and knockdown studies

artículo científico publicado en 2010

Phosphomevalonate kinase is a cytosolic protein in humans

artículo científico publicado en 2004

Slc25a17 Gene Trapped Mice: PMP34 Plays a Role in the Peroxisomal Degradation of Phytanic and Pristanic Acid

scientific article published on 24 March 2020

Lista de obras de

A PEX6-defective peroxisomal biogenesis disorder with severe phenotype in an infant, versus mild phenotype resembling Usher syndrome in the affected parents

A role for the peroxisomal 3-ketoacyl-CoA thiolase B enzyme in the control of PPARα-mediated upregulation of SREBP-2 target genes in the liver.

Age-associated differential microRNA levels in human follicular fluid reveal pathways potentially determining fertility and success of in vitro fertilization.

Expression of calcium-sensing receptor in quail granulosa explants: a key to survival during folliculogenesis

Fine structure of the statocyst sensilla of the mysid shrimp Neomysis integer (Leach, 1814) (Crustacea, Mysidacea)

Human mevalonate pyrophosphate decarboxylase is localized in the cytosol

Human peroxisomal disorders ⬇️

Immunohistochemical demonstration of the amphetamine derivatives 3,4-methylenedioxymethamphetamine (MDMA) and 3,4-methylenedioxyamphetamine (MDA) in human post-mortem brain tissues and the pituitary gland

Inborn errors of metabolism in the biosynthesis and remodelling of phospholipids

Mevalonate kinase is a cytosolic enzyme in humans

Mitochondria in peroxisome-deficient hepatocytes exhibit impaired respiration, depleted DNA, and PGC-1α independent proliferation

Mitochondrial disruption in peroxisome deficient cells is hepatocyte selective but is not mediated by common hepatic peroxisomal metabolites

Mitochondrial mosaics in the liver of 3 infants with mtDNA defects

Modified peroxisomes in primary hepatocyte cultures.

Morphogenesis during molting of the setae in the statocyst sensilla of the mysid shrimp Neomysis integer (Leach, 1814) (crustacea, mysidacea)

Neocortical and cerebellar developmental abnormalities in conditions of selective elimination of peroxisomes from brain or from liver

Peroxisome deficient aP2-Pex5 knockout mice display impaired white adipocyte and muscle function concomitant with reduced adrenergic tone

Peroxisome mosaics.

Peroxisomes during development and in distinct cell types.

Peroxisomes in zebrafish: distribution pattern and knockdown studies

Phosphomevalonate kinase is a cytosolic protein in humans

Slc25a17 Gene Trapped Mice: PMP34 Plays a Role in the Peroxisomal Degradation of Phytanic and Pristanic Acid